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Yao Wang Chi-hui Guo Shu-rong Zhuang Xi-jie Chen Li-qiong Jia Ze-yu Chen Zi-long Xia Zhen Wu 《China Geology》2021,4(2):329-352
In the context of global climate change, geosciences provide an important geological solution to achieve the goal of carbon neutrality, China’s geosciences and geological technologies can play an important role in solving the problem of carbon neutrality. This paper discusses the main problems, opportunities, and challenges that can be solved by the participation of geosciences in carbon neutrality, as well as China’s response to them. The main scientific problems involved and the geological work carried out mainly fall into three categories: (1) Carbon emission reduction technology (natural gas hydrate, geothermal, hot dry rock, nuclear energy, hydropower, wind energy, solar energy, hydrogen energy); (2) carbon sequestration technology (carbon capture and storage, underground space utilization); (3) key minerals needed to support carbon neutralization (raw materials for energy transformation, carbon reduction technology). Therefore, geosciences and geological technologies are needed: First, actively participate in the development of green energy such as natural gas, geothermal energy, hydropower, hot dry rock, and key energy minerals, and develop exploration and exploitation technologies such as geothermal energy and natural gas; the second is to do a good job in geological support for new energy site selection, carry out an in-depth study on geotechnical feasibility and mitigation measures, and form the basis of relevant economic decisions to reduce costs and prevent geological disasters; the third is to develop and coordinate relevant departments of geosciences, organize and carry out strategic research on natural resources, carry out theoretical system research on global climate change and other issues under the guidance of earth system science theory, and coordinate frontier scientific information and advanced technological tools of various disciplines. The goal of carbon neutrality provides new opportunities and challenges for geosciences research. In the future, it is necessary to provide theoretical and technical support from various aspects, enhance the ability of climate adaptation, and support the realization of the goal of carbon peaking and carbon neutrality. 相似文献
154.
地震作用对琼州海峡海缆路由区海底稳定性影向的分析 总被引:1,自引:0,他引:1
以琼州海峡的北海—临高段海缆路由为例,利用计算对比的方法,分析了地震作用下,路由区3m以浅海底土液化或滑移的可能性,评价了路由区海底的稳定性。结果发现,在地震烈度为Ⅶ度的地震作用下,砂性土海底的地震剪应力平均值(0.86kPa,1.72kPa和2.57kPa)小于砂性土的液化剪应力(1.60kPa,3.20kPa和4.81kPa);粘性土海底的地震剪应力平均值(1.25kPa,2.49kPa和3.74kPa)小于粘性土的抗滑剪应力平均值(4.07kPa,4.61kPa和4.49kPa),路由区海底稳定性良好;在地震烈度为Ⅷ度的地震作用下,砂性土海底的地震剪应力平均值(1.73kPa,3.45kPa和5.12kPa)大于砂性土的液化剪应力;粘性土海底的地震剪应力平均值(2.49kPa,4.98kPa和7.47kPa)除表层外,大于粘性土的抗滑剪应力,路由区海底会发生失稳破坏。 相似文献
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156.
YU Hui JIA Yonghong 《地球空间信息科学学报》2006,9(4):298-305
IntroductionVegetation distribution and change is regardedas ani mportant sign of urban environment . Withcity expanding and population increasing, herecomes a series of problems on environment ,andmoreover ,greening ratio is regarded as a stand-ard of ci… 相似文献
157.
水合物地震属性研究的一个基本目标是水合物/游离气含量的估算. 这项工作的难度体现在地震反演具有多解性. 这项工作涉及到地震数据的精细处理、速度分析和BSR界面AVO分析等多个具体环节. 本文继承前人的有关成果,尝试进行了水合物/游离气含量估算方法的研究. 以区域地质、地震和化探等多元方法信息为基础,以定性推断BSR以及BSR界面AVO性质为导向,通过AVO正演模型方法,半定量(或定量)地估算BSR界面上与下地层中水合物/游离气(或水合物/水合物)的含量. 运用这种方法,结合海上有利于天然气水合物的E研究区某测线地震资料,尝试估算了BSR界面之上和之下介质中水合物/游离气的含量. 相似文献
158.
159.
超高强混凝土短柱抗震性能的试验研究 总被引:4,自引:0,他引:4
通过对12根剪跨比λ=2.0的超高强混凝土短柱在低周反复荷载下抗震性能的试验研究,分析了其破坏形态,并研究了轴压比和配箍率对试件滞回特性和抗震延性的影响,提出了满足一定延性要求(μ△≥3.0)超高强混凝土短柱的轴压比限值和箍筋加密区的最小配箍特征值的建议值。该值可为现行规范的修订提供参考。 相似文献
160.
Yun Jiang Piers Koefoed Olga Pravdivtseva Heng Chen Chun‐Hui Li Fang Huang Li‐Ping Qin Jia Liu Kun Wang 《Meteoritics & planetary science》2021,56(1):61-76
The alkali element K is moderately volatile and fluid mobile; thus, it can be influenced by both primary processes (evaporation and recondensation) in the solar nebula and secondary processes (thermal and aqueous alteration) in the parent body. Since these primary and secondary processes would induce different isotopic fractionations, K isotopes could become a potential tracer to distinguish them. Using recently developed methods with improved precision (0.05‰, 95% confidence interval), we systematically measured the K isotopic compositions and major/trace elemental compositions of chondritic components (18 chondrules, 3 CAIs, 2 matrices, and 5 bulks) in the carbonaceous chondrite fall Allende. Among all the components analyzed in this study, CAIs, which formed initially under high‐temperature conditions in the solar nebula and were dominated by nominally K‐free refractory minerals, have the highest K2O content (average 0.53 wt%) and have K isotope compositions most enriched in heavy isotopes (δ41K: ?0.30 to ?0.25‰). Such an observation is consistent with previous petrologic studies that show CAIs in Allende have undergone alkali enrichment during metasomatism. In contrast, chondrules contain lower K2O content (0.003–0.17 wt%) and generally lighter K isotope compositions (δ41K: ?0.87‰ to ?0.24‰). The matrix and bulks are nearly identical in K2O content and K isotope compositions (0.02–0.05 wt%; δ41K: ?0.62 to ? 0.46‰), which are, as expected, right in the middle of CAIs and chondrules. This strongly indicates that most of the chondritic components of Allende suffered aqueous alteration and their K isotopic compositions are the ramification of Allende parent‐body processing instead of primary nebular signatures. Nevertheless, we propose the small K isotope fractionations observed (< 1‰) among Allende components are likely similar to the overall range of K isotopic fractionation that occurred in nebular environment. Furthermore, the K isotope compositions seen in the components of Allende in this study are consistent with MC‐ICP‐MS analyses of the components in ordinary chondrites, which also show an absence of large (10‰) isotope fractionations. This is not expected as evaporation experiments in nebular conditions suggest there should be large K isotopic fractionations. Nevertheless, possible nebular processes such as chondrules back exchanging with ambient gas when they formed could explain this lack of large K isotopic variation. 相似文献